Literature DB >> 8884576

Morphological studies of skeletal muscle in lactic acidosis.

N B Romero1, A Lombès, G Touati, O Rigal, P Frachon, M A Cheval, M Giraud, S Possekel, M Fardeau, H Ogier de Baulny.   

Abstract

This paper underscores the contribution of routine morphological examination of skeletal muscle in patients with lactic acidosis. Mitochondrial disorders are by far the most common causes of primary lactic acidosis, in which muscle biopsy analysis helps in diagnosis and in the search for the molecular anomalies. Thus, we focus our attention on one particular point: the contribution of the morphological study of muscle biopsy in primary lactic acidosis due to mitochondrial disorders, especially mitochondrial respiratory-chain diseases.

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Year:  1996        PMID: 8884576     DOI: 10.1007/bf01799113

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  10 in total

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Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

2.  RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS.

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Journal:  Neurology       Date:  1963-11       Impact factor: 9.910

3.  Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle.

Authors:  N Romero; C Marsac; M Fardeau; M Droste; B Schneyder; B Kadenbach
Journal:  Histochemistry       Date:  1990

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Authors:  M Fardeau
Journal:  Ann Anat Pathol (Paris)       Date:  1973 Jan-Mar

5.  The histochemical characterization of the coupling state of skeletal muscle mitochondria.

Authors:  A E Meijer; A H Vloedman
Journal:  Histochemistry       Date:  1980

6.  Tissue- and species-specific expression of cytochrome c oxidase isozymes in vertebrates.

Authors:  B Kadenbach; A Stroh; A Becker; C Eckerskorn; F Lottspeich
Journal:  Biochim Biophys Acta       Date:  1990-02-02

Review 7.  Mitochondrial encephalomyopathies.

Authors:  S DiMauro; C T Moraes
Journal:  Arch Neurol       Date:  1993-11

Review 8.  Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency.

Authors:  N B Romero; C Marsac; M Paturneau-Jouas; H Ogier; S Magnier; M Fardeau
Journal:  Neuromuscul Disord       Date:  1993-01       Impact factor: 4.296

9.  Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children.

Authors:  S Possekel; A Lombes; H Ogier de Baulny; M A Cheval; M Fardeau; B Kadenbach; N B Romero
Journal:  Histochem Cell Biol       Date:  1995-01       Impact factor: 4.304

10.  Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

Authors:  A M Seligman; M J Karnovsky; H L Wasserkrug; J S Hanker
Journal:  J Cell Biol       Date:  1968-07       Impact factor: 10.539

  10 in total
  2 in total

1.  Mitochondrial respiratory chain defects are not accompanied by an increase in the activities of lactate dehydrogenase or manganese superoxide dismutase in paediatric skeletal muscle biopsies.

Authors:  I P Hargreaves; S J Heales; J M Land
Journal:  J Inherit Metab Dis       Date:  1999-12       Impact factor: 4.982

Review 2.  Mitochondrial oxidative phosphorylation: pitfalls and tips in measuring and interpreting enzyme activities.

Authors:  D Chretien; P Rustin
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

  2 in total

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